(Y06.1) By parent

More details coming soon

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18 303 in individuals diagnosis by parent confirmed
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4 324 deaths with diagnosis by parent
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24% mortality rate associated with the disease by parent

Diagnosis by parent is diagnosed Women are 50.52% more likely than Men

4 528

Men receive the diagnosis by parent

2 940 (64.9 %)

Died from this diagnosis.

100
95
90
85
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75
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65
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55
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15
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5
0
13 775

Women receive the diagnosis by parent

1 384 (10.0 %)

Died from this diagnosis.

Risk Group for the Disease by parent - Men aged 15-19 and Women aged 10-14

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In Men diagnosis is most often set at age 15-24
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Less common in men the disease occurs at Age 0-14, 25-95+Less common in women the disease occurs at Age 0-9, 15-54, 65-95+
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In Women diagnosis is most often set at age 10-14, 55-64

Disease Features by parent

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Absence or low individual and public risk
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By parent - what does this mean

Inheritance of a disease from parent to child occurs when a genetic mutation is passed from one generation to the next, causing the offspring to be born with the condition. this can happen in several ways, such as autosomal dominant inheritance, autosomal recessive inheritance, x-linked inheritance, and mitochondrial inheritance.

What happens during the disease - by parent

The pathogenesis of the disease by parent is a complex process involving genetic, environmental, and epigenetic factors. genetic factors can include inherited mutations in genes that are important for normal development and functioning of the body, while environmental factors can include exposure to toxins, allergens, and infectious agents. epigenetic factors, such as changes in gene expression due to diet, lifestyle, or stress, can also play a role in the development of the disease. all of these factors interact to produce the symptoms and signs seen in the affected individual.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Take a detailed medical history from the parent.
  • Conduct a physical exam of the patient.
  • Order laboratory tests, such as blood work and urine tests.
  • Perform imaging studies, such as X-rays or MRI scans.
  • Prescribe medications to treat the symptoms.
  • Refer the patient to a specialist for further evaluation.
Additions:
  • Perform a genetic test to determine the cause of the disease.
  • Order an electrocardiogram (ECG) to check for heart abnormalities.

Treatment and Medical Assistance

Main Goal: Treat the Disease
  • Ensure the patient takes their prescribed medication as directed.
  • Encourage healthy eating habits.
  • Schedule regular doctor visits.
  • Monitor the patient's symptoms and report any changes to the doctor.
  • Provide emotional support to the patient.
  • Educate the patient about the disease and its treatment.
  • Encourage the patient to engage in physical activity.
  • Ensure the patient gets enough rest.
  • Provide assistance with daily activities, if needed.
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25 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

By parent - Prevention

Parents can help prevent their children from getting the disease by ensuring they receive all necessary vaccinations, practicing good hygiene, such as washing hands regularly, avoiding contact with people who have the disease, and ensuring their children eat a balanced diet with plenty of fruits and vegetables.